| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75523245-75523266 | |||||
| chrX:76172795-76173148 | Rare:67 | ||||
| chrX:77895412-77895739 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78104004-78104320 | Common:4; Rare:116 | ||||
| chrX:81201618-81201869 | Rare:28 | ||||
| chrX:81201876-81202245 | Rare:62 | ||||
| chrX:81202319-81202666 | Common:2; Rare:48 | ||||
| chrX:87517694-87518049 | Common:2; Rare:77 | ||||
| chrX:96684726-96685051 | Rare:53 | ||||
| chrX:100584773-100584940 | Rare:22 | ||||
| chrX:100643852-100644154 | Common:1; Rare:42 | ||||
| chrX:100644157-100644447 | Common:2; Rare:42 | ||||
| chrX:101386150-101386344 | Rare:21 | ||||
| chrX:101407799-101408317 | Common:5; Rare:94; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:103585449-103585671 | Common:3; Rare:45 |